Non-canonical Notch signaling: emerging role and mechanism

被引:175
|
作者
Andersen, Peter [1 ]
Uosaki, Hideki [1 ]
Shenje, Lincoln T. [1 ]
Kwon, Chulan [1 ]
机构
[1] Johns Hopkins Univ, Div Cardiol, Dept Med, Baltimore, MD 21205 USA
关键词
NEURAL CREST FORMATION; BETA-CATENIN; INTRACELLULAR DOMAIN; CELL FATE; TUMOR-SUPPRESSOR; GAMMA-SECRETASE; DROSOPHILA-NOTCH; SULINDAC SULFIDE; PATHWAY; PROTEIN;
D O I
10.1016/j.tcb.2012.02.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Notch is an ancient transmembrane receptor with crucial roles in cell-fate choices. Although the 'canonical' Notch pathway and its core members are well established involving ligand-induced cleavage of Notch for transcriptional regulation - it has been unclear whether Notch can also function independently of ligand and transcription ('non-canonically') through a common mechanism. Recent studies suggest that Notch can non-canonically exert its biological functions by post-translationally targeting Wnt/beta-catenin signaling, an important cellular and developmental regulator. The non-canonical Notch pathway appears to be highly conserved from flies to mammals. Here, we discuss the emerging conserved mechanism and role of ligand/transcription-independent Notch signaling in cell and developmental biology.
引用
收藏
页码:257 / 265
页数:9
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